The following data is part of a premarket notification filed by Elekta Instrument Ab with the FDA for Leksell Stereotactic System, Injection/ Aspiration Needle Kit.
Device ID | K152558 |
510k Number | K152558 |
Device Name: | Leksell Stereotactic System, Injection/ Aspiration Needle Kit |
Classification | Neurological Stereotaxic Instrument |
Applicant | ELEKTA INSTRUMENT AB KUNGSTENSGATAN 18, P.O. BOX 7593 Stockholm, SE Se-103 93 |
Contact | Emma Widmark |
Correspondent | Emma Widmark ELEKTA INSTRUMENT AB KUNGSTENSGATAN 18, P.O. BOX 7593 Stockholm, SE Se-103 93 |
Product Code | HAW |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-09 |
Decision Date | 2016-03-02 |